Replacement of Stoichiometric DDQ with a Low Potential o-Quinone

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Letter Cite This: Org. Lett. XXXX, XXX, XXX−XXX

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Replacement of Stoichiometric DDQ with a Low Potential o‑Quinone Catalyst Enabling Aerobic Dehydrogenation of Tertiary Indolines in Pharmaceutical Intermediates Bao Li, Alison E. Wendlandt,† and Shannon S. Stahl* Department of Chemistry, University of WisconsinMadison, 1101 University Avenue, Madison, Wisconsin 53706, United States

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S Supporting Information *

ABSTRACT: A transition-metal/quinone complex, [Ru(phd)3]2+ (phd = 1,10-phenanthroline-5,6-dione), is shown to be effective for aerobic dehydrogenation of 3° indolines to the corresponding indoles. The results show how low potential quinones may be tailored to provide a catalytic alternative to stoichiometric DDQ, due to their ability to mediate efficient substrate dehydrogenation while also being compatible with facile reoxidation by O2. The utility of the method is demonstrated in the synthesis of key intermediates to pharmaceutically important molecules.

Q

probe enzymatic mechanisms,3−12 while recent studies have expanded on synthetic applications.13−31 These studies show that o-quinones are effective catalysts for aerobic dehydrogenation of primary and secondary amines (Scheme 1b). Primary amines are the native substrates for CAO enzymes, and mechanistic data support a pathway in which amine condensation with the quinone affords an iminoquinone intermediate that undergoes an internal redox reaction via hydride transfer to generate the oxidized substrate (Scheme 1c).3−11 Consistent with this mechanism, biomimetic oquinones often support selective dehydrogenation of 1° amines, without reacting with 2° and 3° amines.16,21,22,24 In complementary efforts, we showed that 1,10-phenanthroline5,6-dione (phd, Scheme 1b), in the presence of ZnI2, can effect catalytic dehydrogenation of 2° amines with O2 as the terminal oxidant.17 This reactivity arises from a different mechanism involving a hemiaminal intermediate (Scheme 1c). Quinone-catalyzed aerobic oxidation of 3° amines has not yet been reported and remains a challenge. For example, the phd/ZnI2 catalyst system showed poor reactivity in the attempted dehydrogenation of a 3° indoline.17 The latter reaction is a valuable target owing to the prevalence of Nsubstituted indoles in bioactive natural products and pharmaceuticals.32−34 Dehydrogenation of indolines provides a strategic route to these compounds,35−38 often overcoming limitations of other synthetic routes to indoles.39−44 Indoline dehydrogenation is typically accomplished with (super)stoichiometric oxidants, such as DDQ (2,3-dichloro-5,6dicyano-1,4-benzoquinone), KMnO4, or MnO2.39,45−47 DDQ has found especially broad use, including application in

uinone cofactors present in copper amine oxidases (CAOs) and other “quinoenzymes” (Scheme 1a) have inspired numerous efforts to mimic their reactivity with synthetic catalysts.1,2 Early efforts used ortho-quinones to

Scheme 1. Quinone-Catalyzed Dehydrogenation of Amines

Received: January 9, 2019

© XXXX American Chemical Society

A

DOI: 10.1021/acs.orglett.9b00111 Org. Lett. XXXX, XXX, XXX−XXX

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Organic Letters process-scale pharmaceutical synthesis.38 The cost, toxicity, and waste disposal associated with DDQ have motivated efforts to identify catalytic alternatives.13,48−52 Herein, we pursue this goal and report the first 3° amine dehydrogenation reactions with CAO-inspired o-quinone catalysts, showing that a phd-ligated Ru complex,18 [Ru(phd)3](PF6)2, enables efficient conversion of 3° indolines to indoles (Scheme 1d). This low-potential o-quinone catalyst system is shown to have broader functional group compatibility than DDQ and outperforms stoichiometric DDQ in the preparation of important pharmaceutical intermediates. The enthalpy of indoline dehydrogenation is ∼12 kcal/mol, and assuming typical entropic contributions, the ΔG° for this reaction is estimated to be ≤5 kcal/mol.53 DDQ is a highpotential quinone that provides an unnecessarily strong driving force for dehydrogenation (>40 kcal/mol).54 We postulated that a lower-potential quinone for indoline dehydrogenation could exhibit broader functional-group compatibility, while also enabling efficient aerobic catalytic turnover (Scheme 2).

Figure 1. Substrate scope of aerobic dehydrogenation of Nsubstituted indolines to indoles. Conditions (A): 1.0 mmol scale, 2.5 mol % [Ru(phd)3](PF6)2, 1 mol % Bu4NI, MeCN (0.1 M), O2, room temperature. Conditions (B): 1.0 mmol scale, 2.5 mol % [Ru(phd)3](PF6)2, 5 mol % Co(salophen), MeOH (0.1 M), O2, 65 °C. Isolated yields. aReactions were run at 65 °C. bReactions were run at 40 °C.

Scheme 2. Quinone-Catalyzed Aerobic Dehydrogenation Process Using Electron-Transfer Mediators (ETMs)56

derivatives 4a and 9a, good product yields were obtained with both catalyst systems. Catalyst system B occasionally led to substrate decomposition and poor yield (e.g., with 1a), but it appears to be the more broadly effective of the two catalyst systems. Simple indoles such as those in Figure 1 are often accessible by other methods, and therefore, the utility of dehydrogenation methods is more evident in complex molecule synthesis. The lower redox potential of the present quinone catalyst relative to DDQ should enable broader functional group compatibility. Substrate 6a, for example, features an oxidatively sensitive pinacolboronate. This substrate underwent dehydrogenation in 80% yield with catalyst system B, while a significantly reduced yield was obtained with stoichiometric DDQ (47% yield, with complete substrate conversion). More extensive testing was conducted by evaluating the dehydrogenation of 2a under catalytic conditions B (cf. Figure 1) and with stoichiometric DDQ in the presence of oxidatively sensitive molecules (Figure 2). Examples include those known to react with DDQ, such as diphenylmethane,58 isochroman,59 and allylic alcohol.60 In each case, 2b was generated in excellent yield under the

Several of the o-quinones in Scheme 1b were analyzed by cyclic voltammetry.55 Q2, phd, and [Ru(phd)3]2+ exhibit reduction potentials of −0.93, −0.88, and −0.59 V, respectively, vs Fc+/ Fc in MeCN. These potentials are 0.73−1.07 V lower than that of DDQ (0.14 V vs Fc+/Fc) under the same conditions. Tertiary amines are unlikely to be capable of generating stable covalent adducts similar to those observed with 1° and 2° amines (cf. Scheme 1c).3−11 Nevertheless, we reasoned that transient adduct formation could lead to kinetically efficient dehydrogenation, even in the absence of the strong thermodynamic driving force available from DDQ. To test our hypothesis, we assessed the reactivity of Q1, Q2, and phd, in combination with various electron-transfer mediators (ETMs), as catalysts for dehydrogenation of 1methylindoline 1a and the more electron-deficient derivative 2a. Two complementary catalyst systems/reaction conditions were identified from these efforts: [Ru(phd)3]2+/Bu4NI/ CH3CN (A) and [Ru(phd)3]2+/Co(salophen)/MeOH57 (B), respectively, for 1a and 1b (see Supporting Information for full screening data). Catalytic conditions A and B were then evaluated with a number of other indoline substrates (Figure 1). The [Ru(phd)3]2+/Bu4NI catalyst system A appears to fare best with electronically neutral substrates. Good yields of indole product were obtained with 1-methylindoline 1a, in addition to derivatives 7a, 8a, 11a, 12a, and 13a bearing modified N-substituents and/or small substituents on the indoline core. More electron-rich substrates, such as 1-methyl5-methoxyindoline 3a and 1-methyl-7-benzyloxyindoline 10a, and more electron-poor derivatives, such as 1-methyl-5bromoindoline 2a and 5-formylindoline 5a, afforded lower yields with this catalyst system. In each of these cases, the [Ru(phd)3]2+/Co(salophen) catalyst system B proved more effective, enabling higher product yields and shorter reaction time. In a few cases, such as the chloro- and cyano-substituted

Figure 2. Competition studies with oxidatively sensitive molecules. B

DOI: 10.1021/acs.orglett.9b00111 Org. Lett. XXXX, XXX, XXX−XXX

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formation of an adduct between the tertiary amine and the phd o-quinone. As expected, however, the 3° amine substrate does not form a resting state adduct with the quinone, as revealed by variable-temperature NMR analysis of a solution of [Ru(phd)3]2+ and 2a.62 To further probe the mechanism of the reaction, deuterium kinetic isotope effects (KIEs) were obtained by independently comparing the rate of dehydrogenation of 2a, 2a-C2-d2, 2a-C3d2, and 2a-d4 (Figure 3a). The data revealed a significant

catalytic aerobic conditions (91−97% yield), with virtually no decomposition of the additive (≥94% recovery). Meanwhile, the reactions with DDQ led to moderate yields of 2b (40−78% yield) and often resulted in significant decomposition of the additive (up to 90%). The preferred reactivity of indoline 2a over N-phenyl pyrrolidine and N-phenyl piperidine may be rationalized by the conformational constraints of the indoline ring, which enforce conjugation with the arene ring and should enhance the hydride donor ability of the substrate. The catalytic conditions obtained here were then evaluated in the preparation of pharmaceutical intermediates (Scheme 3). Indole 16b is an intermediate en route to the natural Scheme 3. Quinone-Catalyzed Dehydrogenation of Pharmaceutical Intermediates

Figure 3. Kinetic isotope effect data from Ru(phd)3]2+/Co(salophen)-catalyzed dehydrogenation of 2a and its isotopologues. (Note: The deuterium labels in the C3 position of 2a-d3 are a byproduct of the synthetic protocol; NaBD3CN/DOAc-mediated reduction of the indole leads to full H/D exchange at the C3 position. Then, partial H incorporation from MeOH occurs at the C3 position during the dehydrogenation reaction.)

product Enzastaurin (Scheme 3), which has been targeted as a PET reagent for imaging of protein kinase C.61 Gram-scale dehydrogenation of indoline 16a with the [Ru(phd)3]2+/ Co(salophen) catalyst system provided 17b in near-quantitative NMR yield (97%; 88% isolated yield), reflecting the excellent chemoselectivity for dehydrogenation of the indoline rather than the tertiary piperidine and also demonstrating compatibility with a pyridine substituent. This result may be compared with a previously reported protocol, which employed 1.1 equiv of DDQ and generated 16b in 68% yield.43 Preparation of the asthma drug candidate LY290154 (Scheme 3) proceeds via the indole intermediate 17b. Reported efforts to carry out N-alkylation of the substituted indole with a secondary alkyl halide were complicated by competing elimination reactions. Therefore, the synthesis of 17b was conducted by sequential alkylation and dehydrogenation of the corresponding indoline with DDQ.38 Use of the [Ru(phd)3]2+/Co(salophen) catalyst system in a gram-scale aerobic dehydrogenation of 17a afforded 17b in 91% isolated yield, again surpassing the reported outcome with stoichiometric DDQ (80% yield). The good reactivity of the low-potential quinone catalyst may be rationalized by a mechanistic variant of the “hemiaminal” mechanism in Scheme 1c, involving transient

deuterium KIE at C2 (KIE = 1.9) but no KIE at the C3 position. An intramolecular competition deuterium KIE of 3.3 was observed at C2, obtained by probing the reaction of 2a-d3 (Figure 3b).63 The higher magnitude of the latter KIE relative to the independent rate KIE suggests that the reaction does not proceed by a single-step bimolecular hydride-transfer pathway, and it is consistent with pre-equilibrium formation of a transient covalent adduct prior to hydride transfer from the C2 position of the indoline. This pathway is consistent with the lack of reactivity exhibited by substrates bearing Ncarbonyl or -sulfonyl substituents (e.g., Ac, Ts; cf. last entry in Figure 1). The latter results could also be rationalized by a single-electron transfer pathway; however, such a pathway is unlikely, considering the oxidative peak potentials of Nmethylindolines 1a and 2a are nearly 1 V higher than the potential of [Ru(phd)3]2+ (approximately +0.40 V vs −0.59 V, respectively). The catalyst system described here should find application in other tertiary amine dehydrogenation reactions. An important example is cross-dehydrogenative coupling (CDC) for functionalization adjacent to the nitrogen atom.64,65 As a preliminary test of this application, we evaluated the [Ru(phd)3]2+/Co(salophen) catalyst system in the reaction of N-phenyltetrahydroisoquinoline with a series of different C

DOI: 10.1021/acs.orglett.9b00111 Org. Lett. XXXX, XXX, XXX−XXX

Organic Letters nucleophiles (Scheme 4). Excellent yields were obtained in C− C bond forming reactions with diethylmalonate, 4-hydroxy-

ACKNOWLEDGMENTS

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REFERENCES

(1) Anthony, C.; Ghosh, M.; Blake, C. C. F. The Structure and Function of Methanol Dehydrogenase and Related Quinoproteins Containing Pyrrolo-quinoline Quinone. Biochem. J. 1994, 304, 665− 674. (2) Anthony, C. Quinoprotein-Catalysed Reactions. Biochem. J. 1996, 320, 697−711. (3) Eckert, T. S.; Bruice, T. C. Chemical Properties of Phenanthrolinequinones and The Mechanism of Amine Oxidation by o-Quinones of Medium Redox Potentials. J. Am. Chem. Soc. 1983, 105, 4431−4441. (4) Sleath, P. R.; Noar, J. B.; Eberlein, G. A.; Bruice, T. C. Synthesis of 7,9-Didecarboxymethoxatin (4,5-dihydro-4,5-dioxo-1H-pyrrolo[2,3-f ] quinoline-2-carboxylic acid) and Comparison of Its Chemical Properties with Those of Methoxatin and Analogous o-Auinones. Model Studies Directed Toward the Action of PQQ Requiring Bacterial Oxidoreductases and Mammalian Plasma Amine Oxidase. J. Am. Chem. Soc. 1985, 107, 3328−3338. (5) Mure, M.; Klinman, J. P. Model Studies of TopaquinoneDependent Amine Oxidases. 1. Oxidation of Benzylamine by Topaquinone Analogs. J. Am. Chem. Soc. 1995, 117, 8698−8706. (6) Mure, M.; Klinman, J. P. Model studies of TopaquinoneDependent Amine Oxidases. 2. Characterization of Reaction Intermediates and Mechanism. J. Am. Chem. Soc. 1995, 117, 8707− 8718. (7) Lee, Y.; Sayre, L. M. Model Reactions for the QuinoneContaining Copper Amine Oxidases. Anaerobic Reaction Pathways and Catalytic Aerobic Deamination of Activated Amines in Buffered Aqueous Acetonitrile. J. Am. Chem. Soc. 1995, 117, 3096−3105. (8) Lee, Y.; Sayre, L. M. Model Studies on the Quinone-Containing Copper Amine Oxidases. Unambiguous Demonstration of a Transamination Mechanism. J. Am. Chem. Soc. 1995, 117, 11823−11828. (9) Itoh, S.; Ogino, M.; Haranou, S.; Terasaka, T.; Ando, T.; Komatsu, M.; Ohshiro, Y.; Fukuzumi, S.; Kano, K. A Model Compound of the Novel Cofactor Tryptophan Tryptophylquinone of Bacterial Methylamine Dehydrogenases. Synthesis and Physicochemical Properties. J. Am. Chem. Soc. 1995, 117, 1485−1493. (10) Itoh, S.; Takada, N.; Haranou, S.; Ando, T.; Komatsu, M.; Ohshiro, Y.; Fukuzumi, S. Model Studies of TTQ-Containing Amine Dehydrogenases. J. Org. Chem. 1996, 61, 8967−8974. (11) Ling, K.-Q.; Kim, J.; Sayre, L. M. Catalytic Turnover of Benzylamine by a Model for the Lysine Tyrosylquinone (LTQ) Cofactor of Lysyl Oxidase. J. Am. Chem. Soc. 2001, 123, 9606−9611. (12) For a related recent study of biomimetic o-quinone-catalyzed oxidation of alcohols, see: McSkimming, A.; Cheisson, T.; Carroll, P. J.; Schelter, E. J. Functional Synthetic Model for the LanthanideDependent Quinoid Alcohol Dehydrogenase Active Site. J. Am. Chem. Soc. 2018, 140, 1223−1226. (13) See the following for a review of quinone-catalyzed oxidation reactions. (For additional reviews of quinone-catalyzed oxidation of amines, see refs 14 and 15.) Wendlandt, A. E.; Stahl, S. S. QuinoneCatalyzed Selective Oxidation of Organic Molecules. Angew. Chem., Int. Ed. 2015, 54, 14638−14658. (14) Largeron, M. Protocols for the Catalytic Oxidation of Primary Amines to Imines. Eur. J. Org. Chem. 2013, 2013, 5225−5235. (15) Largeron, M.; Fleury, M.-B. Aerobic Catalytic Systems Inspired by Copper Amine Oxidases: Recent Developments and Synthetic Applications. Org. Biomol. Chem. 2017, 15, 4722−4730. (16) Wendlandt, A. E.; Stahl, S. S. Chemoselective Organocatalytic Aerobic Oxidation of Primary Amines to Secondary Imines. Org. Lett. 2012, 14, 2850−2853.

a

1.0 mmol scale. Yields were determined by 1H NMR. Isolated yields in parentheses.

coumarin, and indole. These results set the stage for future studies to explore other aerobic oxidative coupling reactions with CAO-inspired quinone catalyst systems. In summary, here we have demonstrated that a CAOinspired o-quinone catalyst, [Ru(phd)3]2+, is effective for the aerobic dehydrogenation of 3° indolines. These observations represent an important advance beyond the established reactivity of CAO catalyst systems with 1° and 2° amines. The low-potential nature of quinone catalyst systems of this type provides the basis for excellent functional-group compatibility and establishes a foundation for the development of other catalytic alternatives to stoichiometric DDQ and related high-potential oxidants, with applications including dehydrogenation and oxidative coupling reactions.

ASSOCIATED CONTENT

S Supporting Information *

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.orglett.9b00111. Experimental procedures and characterization data for all compounds (PDF)

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Financial support was provided by the NIH (R01 GM100143). Spectroscopic instrumentation was partially supported by the NIH (S10 OD020022-1) and the NSF (CHE-1048642).

Scheme 4. Quinone-Catalyzed Cross-Dehydrogenative Coupling (CDC) Reactions of NPhenyltetrahydroisoquinolinea

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Letter

AUTHOR INFORMATION

Corresponding Author

*E-mail: [email protected]. ORCID

Alison E. Wendlandt: 0000-0003-2970-9817 Shannon S. Stahl: 0000-0002-9000-7665 Present Address †

Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Ave, Cambridge, MA 02139, USA. E-mail: [email protected].

Author Contributions

The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript. Notes

The authors declare no competing financial interest. D

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(37) Baran, P. S.; Guerrero, C. A.; Corey, E. J. Short, Enantioselective Total Synthesis of Okaramine N. J. Am. Chem. Soc. 2003, 125, 5628−5629. (38) Merschaert, A.; Boquel, P.; Van Hoeck, J. P.; Gorissen, H.; Borghese, A.; Bonnier, B.; Mockel, A.; Napora, F. Novel Approaches towards the LTD4/E4 Antagonist, LY290154. Org. Process Res. Dev. 2006, 10, 776−783. (39) For reviews, see the following and refs 40−44. Karchava, A. V.; Melkonyan, F. S.; Yurovskaya, M. A. New strategies for the Synthesis of N-Alkylated Indoles (Review). Chem. Heterocycl. Compd. 2012, 48, 391−407. (40) Gribble, G. W. Recent Developments in Indole Ring SynthesisMethodology and Applications. J. Chem. Soc., Perkin Trans. 2000, 1, 1045−1075. (41) Humphrey, G. R.; Kuethe, J. T. Practical Methodologies for the Synthesis of Indoles. Chem. Rev. 2006, 106, 2875−2911. (42) Taber, D. F.; Tirunahari, P. K. Indole Synthesis: A Review and Proposed Classification. Tetrahedron 2011, 67, 7195−7210. (43) Vicente, R. Recent Advances in Indole Syntheses: New Routes for a Classic Target. Org. Biomol. Chem. 2011, 9, 6469−6480. (44) Gribble, G. W. Indoline Dehydrogenation. Indole Ring Synthesis: From Natural Products to Drug Discovery, 1st ed.; John Wiley & Sons, Ltd.: West Sussex, U.K., 2016; pp 539−552. (45) For examples of recent, catalytic indoline dehydrogenation methods, see the following and refs 46 and 47: Reddy, K. H. V.; Satish, G.; Ramesh, K.; Karnakar, K.; Nageswar, Y. V. D. An Efficient Synthesis of N-Substituted Indoles from Indoline/Indoline Carboxylic Acid via Aromatization Followed by C-N Cross-Coupling Reaction by Using Nano Copper Oxide as a Recyclable Catalyst. Tetrahedron Lett. 2012, 53, 3061−3065. (46) Peng, F.; McLaughlin, M.; Liu, Y.; Mangion, I.; Tschaen, D. M.; Xu, Y. A Mild Cu(I)-Catalyzed Oxidative Aromatization of Indolines to Indoles. J. Org. Chem. 2016, 81, 10009−10015. (47) Yayla, H. G.; Peng, F.; Mangion, I. K.; McLaughlin, M.; Campeau, L.-C.; Davies, I. W.; DiRocco, D. A.; Knowles, R. R. Discovery and Mechanistic Study of a Photocatalytic Indoline Dehydrogenation for the Synthesis of Elbasvir. Chem. Sci. 2016, 7, 2066−2073. (48) For certain reactions, DDQ may be used as a catalyst in combination with cocatalysts, such as NOx species, to enable O2 to serve as the stoichiometric oxidant. These protocols are not universally applicable, however, and were significantly less effective in the reactions reported here. For examples of DDQ/NOx cocatalysis, see refs 49−52. (49) Shen, Z.; Dai, J.; Xiong, J.; He, X.; Mo, W.; Hu, B.; Sun, N.; Hu, X. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)/tert-Butyl Nitrite/Oxygen: A Versatile Catalytic Oxidation System. Adv. Synth. Catal. 2011, 353, 3031−3038. (50) Wang, L.; Li, J.; Yang, H.; Lv, Y.; Gao, S. Selective Oxidation of Unsaturated Alcohols Catalyzed by Sodium Nitrite and 2,3-Dichloro5,6-dicyano-1,4-benzoquinone with Molecular Oxygen under Mild Conditions. J. Org. Chem. 2012, 77, 790−794. (51) Walsh, K.; Sneddon, H. F.; Moody, C. J. Solar Photochemical Oxidations of Benzylic and Allylic Alcohols Using Catalytic OrganoOxidation with DDQ: Application to Lignin Models. Org. Lett. 2014, 16, 5224−5227. (52) Lancefield, C. S.; Ojo, O. S.; Tran, F.; Westwood, N. J. Isolation of Functionalized Phenolic Monomers through Selective Oxidation and C-O Bond Cleavage of the β-O-4 Linkages in Lignin. Angew. Chem., Int. Ed. 2015, 54, 258−262. (53) See the following reference for a ΔH value; an entropy of 30 e.u. is estimated for the product of two molecules from one: Dean, D.; Davis, B.; Jessop, P. J. The Effect of Temperature, Catalyst and Sterics on the Rate of N-heterocycle Dehydrogenation for Hydrogen Storage. New J. Chem. 2011, 35, 417−422. (54) DDQ + 2e− + 2H+ → DDQH2; ΔE° = 0.89 V vs NHE (ΔG° = 41 kcal/mol). For DDQ reduction potential, see: Huynh, M. T.; Anson, C. W.; Cavell, A. C.; Stahl, S. S.; Hammes-Schiffer, S. Quinone 1 e− and 2 e−/2 H+ Reduction Potentials: Identification and Analysis

(17) Wendlandt, A. E.; Stahl, S. S. Bioinspired Aerobic Oxidation of Secondary Amines and Nitrogen Heterocycles with a Bifunctional Quinone Catalyst. J. Am. Chem. Soc. 2014, 136, 506−512. (18) Wendlandt, A. E.; Stahl, S. S. Modular o-Quinone Catalyst System for Dehydrogenation of Tetrahydroquinolines under Ambient Conditions. J. Am. Chem. Soc. 2014, 136, 11910−11913. (19) Corey, E. J.; Achiwa, K. Oxidation of Primary Amines to Ketones. J. Am. Chem. Soc. 1969, 91, 1429−1432. (20) Largeron, M.; Fleury, M.-B. Oxidative Deamination of Benzylamine by Electrogenerated Quinonoid Systems as Mimics of Amine Oxidoreductases Cofactors. J. Org. Chem. 2000, 65, 8874− 8881. (21) Largeron, M.; Neudorffer, A.; Fleury, M.-B. Oxidation of Unactivated Primary Aliphatic Amines Catalyzed by an Electrogenerated 3,4-Azaquinone Species: A Small-Molecule Mimic of Amine Oxidases. Angew. Chem., Int. Ed. 2003, 42, 1026−1029. (22) Largeron, M.; Chiaroni, A.; Fleury, M.-B. Environmentally Friendly Chemoselective Oxidation of Primary Aliphatic Amines by Using a Biomimetic Electrocatalytic System. Chem. - Eur. J. 2008, 14, 996−1003. (23) Yuan, H.; Yoo, W. J.; Miyamura, H.; Kobayashi, S. Discovery of a Metalloenzyme-like Cooperative Catalytic System of Metal Nanoclusters and Catechol Derivatives for the Aerobic Oxidation of Amines. J. Am. Chem. Soc. 2012, 134, 13970−13973. (24) Largeron, M.; Fleury, M.-B. A Biologically Inspired CuI/ Topaquinone-Like Co-Catalytic System for the Highly AtomEconomical Aerobic Oxidation of Primary Amines to Imines. Angew. Chem., Int. Ed. 2012, 51, 5409−5412. (25) Jawale, D. V.; Gravel, E.; Villemin, E.; Shah, N.; Geertsen, V.; Namboothiri, I. N. N.; Doris, E. Co-Catalytic Oxidative Coupling of Primary Amines to Imines Using an Organic Nanotube-Gold Nanohybrid. Chem. Commun. 2014, 50, 15251−15254. (26) Qin, Y.; Zhang, L.; Lv, J.; Luo, S.; Cheng, J.-P. Bioinspired Organocatalytic Aerobic C-H Oxidation of Amines with an orthoQuinone Catalyst. Org. Lett. 2015, 17, 1469−1472. (27) Leon, M. A.; Liu, X.; Phan, J. H.; Clift, M. D. Amine Functionalization through Sequential Quinone-Catalyzed Oxidation/ Nucleophilic Addition. Eur. J. Org. Chem. 2016, 2016, 4508−4515. (28) Goriya, Y.; Kim, H. Y.; Oh, K. o-Naphthoquinone-Catalyzed Aerobic Oxidation of Amines to (Ket)imines: A Modular Catalyst Approach. Org. Lett. 2016, 18, 5174−5177. (29) Rong, H. J.; Cheng, Y. F.; Liu, F. F.; Ren, S. J.; Qu, J. Synthesis of γ-Lactams by Mild, o-Benzoquinone-Induced Oxidation of Pyrrolidines Containing Oxidation-Sensitive Functional Groups. J. Org. Chem. 2017, 82, 532−540. (30) Largeron, M.; Fleury, M.-B. A Bioinspired Organocatalytic Cascade for the Selective Oxidation of Amines under Air. Chem. - Eur. J. 2017, 23, 6763−6767. (31) Golime, G.; Bogonda, G.; Kim, H. Y.; Oh, K. Biomimetic Oxidative Deamination Catalysis via ortho-Naphthoquinone-Catalyzed Aerobic Oxidation Strategy. ACS Catal. 2018, 8, 4986−4990. (32) Sundberg, R. J. In Indoles; Katritzky, A., Meth-Cohn, O., Rees, C., Eds.; Academic Press: London, U.K., 1996. (33) Kochanowska-Karamyan, A. J.; Hamann, M. T. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety. Chem. Rev. 2010, 110, 4489−4497. (34) Vitaku, E.; Smith, D. T.; Njardarson, J. T. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals. J. Med. Chem. 2014, 57, 10257−10274. (35) Sugiyama, H.; Yokokawa, F.; Aoyama, T.; Shioiri, T. Synthetic studies of N-reverse Prenylated Indole. An efficient Synthesis of Antifungal Indole Alkaloids and N-Reverse Prenylated Tryptophan. Tetrahedron Lett. 2001, 42, 7277−7280. (36) Sugiyama, H.; Shioiri, T.; Yokokawa, F. Syntheses of Four Unusual Amino Acids, Constituents of Cyclomarin A. Tetrahedron Lett. 2002, 43, 3489−3492. E

DOI: 10.1021/acs.orglett.9b00111 Org. Lett. XXXX, XXX, XXX−XXX

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Organic Letters of Deviations from Systematic Scaling Relationships. J. Am. Chem. Soc. 2016, 138, 15903−15910. (55) See Table S1, Figures S1, and S2 in the Supporting Information for details. (56) Piera, J.; Bäckvall, J. E. Catalytic Oxidation of Organic Substrates by Molecular Oxygen and Hydrogen Peroxide by Multistep Electron Transfer-A Biomimetic Approach. Angew. Chem., Int. Ed. 2008, 47, 3506−3523. (57) MeOH was shown to be an especially effective solvent for Co(salophen)/quinone reactivity: Anson, C. W.; Ghosh, S.; HammesSchiffer, S.; Stahl, S. S. Co(salophen)-Catalyzed Aerobic Oxidation of p-Hydroquinone: Mechanism and Implications for Aerobic Oxidation Catalysis. J. Am. Chem. Soc. 2016, 138, 4186−4193. (58) Yi, H.; Liu, Q.; Liu, J.; Zeng, Z.; Yang, Y.; Lei, A. DDQCatalyzed Oxidative C-O Coupling Of sp3 C-H Bonds with Carboxylic Acids. ChemSusChem 2012, 5, 2143−2146. (59) Muramatsu, W.; Nakano, K. Organocatalytic Approach for C(sp3)-H Bond Arylation, Alkylation, and Amidation of Isochromans under Facile Conditions. Org. Lett. 2014, 16, 2042−2045. (60) Cosner, C. C.; Cabrera, P. J.; Byrd, K. M.; Thomas, A. M. A.; Helquist, P. Selective Oxidation of Benzylic and Allylic Alcohols Using Mn(OAc)3/Catalytic 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone. Org. Lett. 2011, 13, 2071−2073. (61) Wang, M.; Xu, L.; Gao, M.; Miller, K. D.; Sledge, G. W.; Zheng, Q. H. [11C]Enzastaurin, The First Design and Radiosynthesis of a New Potential PET Agent for Imaging of Protein Kinase C. Bioorg. Med. Chem. Lett. 2011, 21, 1649−1653. (62) See Supporting Information for more details about the lowtemperature NMR experiments to investigate the interaction between primary, secondary, and tertiary amines with quinone. (63) See ref 26 for a primary KIE of 2.9 observed via independent rate comparison in the quinone-mediated dehydrogenation of a primary amine. And, a large intramolecular competition KIE of 6.4 was reported in ref 17 for the dehydrogenation of a secondary amine. (64) For reviews of CDC reactions, see the following and ref 65: Li, C.-J. Cross-Dehydrogenative Coupling (CDC): Exploring C-C Bond Formations beyond Functional Group Transformations. Acc. Chem. Res. 2009, 42, 335−344. (65) Yeung, C. S.; Dong, V. M. Catalytic Dehydrogenative CrossCoupling: Forming Carbon-Carbon Bonds by Oxidizing Two Carbon-Hydrogen Bonds. Chem. Rev. 2011, 111, 1215−1292.

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DOI: 10.1021/acs.orglett.9b00111 Org. Lett. XXXX, XXX, XXX−XXX